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61098-04-2

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61098-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61098-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,9 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61098-04:
(7*6)+(6*1)+(5*0)+(4*9)+(3*8)+(2*0)+(1*4)=112
112 % 10 = 2
So 61098-04-2 is a valid CAS Registry Number.

61098-04-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chlorobenzylideneamino)-1,2-dihydro-1,5-dimethyl-2-phenylpyrazol-3-one

1.2 Other means of identification

Product number -
Other names 4-Chlorbenzaldehyd-4-aminoantipyrin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61098-04-2 SDS

61098-04-2Relevant articles and documents

Pyrazolone incorporating amino acid metallointercalators as effective DNA targets: Synthesis and in vitro biocidal evaluation

Raman, Natarajan,Selvaganapathy, Muthusamy

, p. 114 - 120 (2013)

Three novel mixed-ligand complexes using pyrazolone derivative (4-chloro-benzylidene-4-aminoantipyrine) as primary ligand and l-methionine as co-ligand, were synthesized and characterized by physico-chemical analytical techniques. The DNA interaction of t

Antipyrine cationic surfactants capping silver nanoparticles as potent antimicrobial agents against pathogenic bacteria and fungi

Aiad,Marzouk, Magda I.,Shaker, Soheir A.,Ebrahim, Nagwa E.,Abd-Elaal, Ali A.,Tawfik, Salah M.

, p. 572 - 583 (2017)

Development of effective anti-microbial agents has been hindered by the emergence of bacterial strains with multi-drug resistance. In this article, we report an efficient synthesis of silver nanoparticle (AgNP) by capping with a synthetic cationic surfact

Synthesis and biological evaluation of new pyrazolone Schiff bases as monoamine oxidase and cholinesterase inhibitors

Tok, Fatih,Ko?yi?it-Kaymak??o?lu, Bedia,Sa?l?k, Begüm Nurpelin,Levent, Serkan,?zkay, Yusuf,Kaplanc?kl?, Zafer As?m

, p. 41 - 50 (2018/11/27)

In the current work, Schiff base derivatives of antipyrine were synthesized. The chemical characterization of the compounds was confirmed using IR, 1H NMR, 13C NMR and mass spectroscopies. The inhibitory potency of synthesized compounds was investigated towards acetylcholinesterase (AChE), butyrylcholinesterase (BuChE), and monoamine oxidases A and B (MAO-A and MAO-B) enzymes. Some of the compounds displayed significant inhibitory activity against AChE and MAO-B enzymes, respectively. According to AChE enzyme inhibition assay, compounds 3e and 3g were found as the most potent derivatives with IC50 values of 0.285 μM and 0.057 μM, respectively. Also, compounds 3a (IC50 = 0.114 μM), 3h (IC50 = 0.049 μM), and 3i (IC50 = 0.054 μM) were the most active derivatives against MAO-B enzyme activity. So as to understand inhibition type, enzyme kinetics studies were carried out. Furthermore, molecular docking studies were performed to define and evaluate the interaction mechanism between compounds 3g and 3h and related enzymes. ADME (Absorption, Distribution, Metabolism, and Excretion) and BBB (Blood, Brain, Barier) permeability predictions were applied to estimate pharmacokinetic profiles of synthesized compounds.

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